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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3860275copy number variation131estd219human GRCh37 chr10: 38,818,427-38,907,931 , GRCh38.p12 chr10: 38,529,499-38,614,800 ABCD1P2
    esv3834770copy number variation743estd219human GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4|NW_003315915.1: 272,024-340,593 , GRCh38.p12 chr4: 34,779,695-34,848,264 LOC105378262
    esv3872670copy number variation646estd219human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    esv3853507copy number variation1095estd219human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3834769copy number variation743estd219human GRCh37 chr4: 34,779,933-34,828,997 , GRCh38.p12 chr4|NW_003315915.1: 270,640-319,704 , GRCh38.p12 chr4: 34,778,311-34,827,375 LOC105378262
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3870498copy number variation1037estd219human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3871990copy number variation8estd219human GRCh37 chr13: 110,732,474-110,761,471 , GRCh38.p12 chr13: 110,080,127-110,109,124 RN7SL783P
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3851668copy number variation544estd219human GRCh37 chr7: 141,765,307-141,792,849 , GRCh38.p12 chr7|NT_187562.1: 27,387-54,929 , GRCh38.p12 chr7: 142,065,507-142,093,049 MGAM
    esv3831165copy number variation113estd219human GRCh37 chr3: 89,394,090-89,418,661 , GRCh38.p12 chr3: 89,344,940-89,369,511 EPHA3
    esv3871992copy number variation8estd219human GRCh37 chr13: 110,740,960-110,763,627 , GRCh38.p12 chr13: 110,088,613-110,111,280 RN7SL783P
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3833727copy number variation624estd219human GRCh37 chr3: 195,456,936-195,471,412 , GRCh38.p12 chr3|NT_187688.1: 50,160-64,603 , GRCh38.p12 chr3|NT_187689.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187690.1: 50,159-64,610 , GRCh38.p12 chr3|NT_187691.1: 50,266-64,780 , GRCh38.p12 chr3|NT_187532.1: 100,562-115,038 , GRCh38.p12 chr3: 195,730,065-195,744,541 , GRCh38.p12 chr3|NT_187678.1: 51,460-65,948 , GRCh38.p12 chr3|NT_187649.1: 50,164-64,603 MUC20
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3850618copy number variation797estd219human GRCh37 chr7: 100,327,251-100,341,280 , GRCh38.p12 chr7: 100,729,628-100,743,657 ZAN
    esv3890498copy number variation1565estd219human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
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